LDH info

Canonical Allele Identifier: CA13432330
Gene: PKNOX2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12273350

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.125371150G>A , CM000673.2:g.125371150G>A GRCh38
NC_000011.9:g.125241046G>A , CM000673.1:g.125241046G>A GRCh37
NC_000011.8:g.124746256G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_022062.2:c.227+3165G>A VV NP_071345.2:p.=
XM_005271642.1:c.227+3165G>A XP_005271699.1:p.=
XM_005271643.1:c.140+3165G>A XP_005271700.1:p.=
XM_006718894.1:c.-1+3165G>A XP_006718957.1:p.=
XM_011542944.1:c.227+3165G>A XP_011541246.1:p.=
XM_011542945.1:c.227+3165G>A XP_011541247.1:p.=
XM_011542946.1:c.227+3165G>A XP_011541248.1:p.=
XM_011542947.1:c.-1+3165G>A XP_011541249.1:p.=
XM_005271642.2:c.227+3165G>A XP_005271699.1:p.=
XM_006718894.2:c.-1+3165G>A XP_006718957.1:p.=
XM_011542945.2:c.227+3165G>A XP_011541247.1:p.=
XM_011542947.2:c.-1+3165G>A XP_011541249.1:p.=
XM_017018110.1:c.227+3165G>A XP_016873599.1:p.=
XM_017018111.1:c.-1+3165G>A XP_016873600.1:p.=
XM_024448643.1:c.227+3165G>A XP_024304411.1:p.=
XM_024448644.1:c.227+3165G>A XP_024304412.1:p.=
XM_024448645.1:c.227+3165G>A XP_024304413.1:p.=
XM_024448646.1:c.227+3165G>A XP_024304414.1:p.=
XM_024448647.1:c.227+3165G>A XP_024304415.1:p.=
XM_024448648.1:c.140+3165G>A XP_024304416.1:p.=
XM_024448649.1:c.140+3165G>A XP_024304417.1:p.=
XM_024448650.1:c.140+3165G>A XP_024304418.1:p.=
XM_024448651.1:c.140+3165G>A XP_024304419.1:p.=
NM_022062.3:c.227+3165G>A VV NP_071345.2:p.=
ENST00000298282.13:c.227+3165G>A ENSP00000298282.8:p.=
ENST00000530517.5:n.408+3165G>A
ENST00000531116.5:n.329+3165G>A
ENST00000532623.5:c.88-14401G>A ENSP00000434377.1:p.=
ENST00000557814.5:n.369+3165G>A
ENST00000558705.1:c.227+3165G>A ENSP00000453374.1:p.=
ENST00000558729.5:n.562+3165G>A
ENST00000559662.5:n.478+3165G>A
ENST00000561298.1:n.453+3165G>A